Artigo

Brain imaging and genetic risk in the pediatric population, Part 2 congenital malformations of the central nervous system

Themis Maria Felix, Maria Gabriela Longo, PATRÍCIA ASHTON PROLLA, LEONARDO MODESTI VEDOLIN

Neuroimaging Clinics of North America, v. 25, n. 1, p. 53-67, 2015.

Motivo: Produção Colaborador HMV

Setor HMV: UDI - Gerência

Área da saúde: Pediatria

Resumo: In this article, an update is presented of the correlation of imaging and genetic findings in congenital malformations of the central nervous system (CMCNS). A nonsystematic search of the PubMed/Medline database was performed. The congenital disorders were classified in 3 groups of malformation: ventral induction disorders, cortical malformations, and congenital malformations of the posterior fossa. The highlights of genotype-imaging phenotype correlation of some congenital malformations are provided. It is hoped that developments in genotype-MR phenotype in CMCNS will foster further prognostic and pathogenic breakthroughs for the frequently associated neurologic dysfunction in children affected by these common diseases.

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